Primary Site >> Stomach Cancer

Gene >> USO1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000514213
Start 75793867:75793867(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1418C>A
AA Mutation p.Ser473Tyr(p.S473Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000514213
Start 75810432:75810432(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199810995
CDS Mutation c.2476G>A
AA Mutation p.Ala826Thr(p.A826T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000514213
Start 75813230:75813230(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2824T>A
AA Mutation p.Ser942Thr(p.S942T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000514213
Start 75774680:75774680(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.560T>C
AA Mutation p.Val187Ala(p.V187A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000514213
Start 75810446:75810446(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2490G>T
AA Mutation p.Glu830Asp(p.E830D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000514213
Start 75774679:75774679(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746800563
CDS Mutation c.559G>A
AA Mutation p.Val187Ile(p.V187I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000514213
Start 75801152:75801152(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1938A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000514213
Start 75724843:75724843(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.29delG
AA Mutation p.Gly10ValfsTer21(p.G10Vfs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000514213
Start 75804132:75804132(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1987-2A>T
Mutation Classification Splice_Site
Feature Type Transcript